Canonical Allele Identifier: PA916009191
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 193561
ClinVar RCV Id: RCV000419557 RCV000675103
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Gln333Glu
CA239095
NM_013976.3:c.997C>G